9,631 reports of this reaction
3.1% of all RANITIDINE reports
#7 most reported adverse reaction
INCORRECT DOSE ADMINISTERED is the #7 most commonly reported adverse reaction for RANITIDINE, manufactured by Ajanta Pharma USA Inc.. There are 9,631 FDA adverse event reports linking RANITIDINE to INCORRECT DOSE ADMINISTERED. This represents approximately 3.1% of all 308,223 adverse event reports for this drug.
RANITIDINE has an overall safety score of 95 out of 100. Patients taking RANITIDINE who experience incorrect dose administered should discuss this symptom with their healthcare provider to determine whether it may be related to their medication and what alternatives may be available.
INCORRECT DOSE ADMINISTERED is moderately reported among RANITIDINE users, representing a notable but not dominant share of adverse events.
In addition to incorrect dose administered, the following adverse reactions have been reported for RANITIDINE:
The following drugs have also been linked to incorrect dose administered in FDA adverse event reports:
INCORRECT DOSE ADMINISTERED has been reported as an adverse event in 9,631 FDA reports for RANITIDINE. This does not prove causation, but indicates an association observed in post-market surveillance data.
INCORRECT DOSE ADMINISTERED accounts for approximately 3.1% of all adverse event reports for RANITIDINE, making it a notable side effect.
If you experience incorrect dose administered while taking RANITIDINE, contact your healthcare provider. They can evaluate whether the symptom is related to your medication and discuss potential adjustments to your treatment plan. Do not stop taking prescribed medication without consulting your doctor.